Biodegradation of 3,5-dinitrosalicylic acid by Phanerochaete chrysosporium
DOI:
https://doi.org/10.1515/fobio-2017-0005Keywords:
nitroaromatic compounds, white-rot fungi, fungal biodegradationAbstract
Despite intensive efforts put on prevention of environment pollution by nitroaromatic compounds, these xenobiotics have not been eliminated from the biosphere. The physicochemical properties make nitroaromatics extremely recalcitrant to biodegradation. Therefore, microbial degraders of these pollutants are sought after. This paper reports preliminary results of the study on degradation of 3,5-dinitrosalicylic acid (DNS) by a basidiomycetous fungus Phanerochaete chrysosporium under stationary conditions in a culture medium containing 0.05–0.5% v/v of DNS. The results obtained suggest that the fungus degrades DNS through the reductive pathway.
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Anasonye, F., Winquist, E., Räsänen, M. 2015. Bioremediation of TNT contaminated soil with fungi under laboratory and pilot scale conditions. International Biodeterioration, 105: 7–12.
Google Scholar
Apelblat, A., Manzurola, E. 1999. Solubilities of o-acetylsalicylic, 4-aminosalicylic, 3,5-dinitrosalicylic, and p-toluic acid, and magnesium- DL -aspartate in water from T’s ( 278 to 348) K. Journal of Chemical Thermodynamics, 31: 85–91.
Google Scholar
Bayman, P., Radkar, G. 1997. Transformation and Tolerance of TNT(2,4,6-trinitrotoluene) by Fungi. International Biodeterioration and Biodegradation, 39: 45–53.
Google Scholar
Bonnarme, P., Jeffries, T.W. 1990. Mn(II) regulation of lignin peroxidases and manganese-dependent peroxidases from lignin-degrading white rot fungi. Applied Environmental Microbiology, 56: 210–217.
Google Scholar
Claus, H. 2013 Microbial degradation of 2,4,6-Trinitrotoluene in vitro and in natural environments. Environmental science and engineering biological remediation of explosive residues. Environmental Science and Engineering, 15–38.
Google Scholar
Cvancarova, M., Kfesinova, Z.,Filipova, A., Covino, S., Cajthami, T. 2012. Biodegradation of PCBs by ligninolytic fungi and characterization of the degradation products. Chemosphere, 88: 1317–1323.
Google Scholar
Fnu, A.,Brzonova, I., Voeller, K., Kozilak, E., Kubatova, A., Yao B., Ji, Y. 2016 Biodegradation of lignin by fungi, bacteria and laccases. Bioresource Technology, 220: 414–424.
Google Scholar
Gong, P., Kuperman, R.G., Sunahara, G.I. 2003. Genotoxicity of 2,5-and 2,6-dinitrotoluene as measured by Tradescantia micronucleus (Trad-MN) bioassay. Mutation Research, 538: 13–18.
Google Scholar
Grundlingh, J., Dargan, P., El-Zanfaly, M., Wood, D. 2011. 2,4-Dinitrophenol (DNP): A weight loss agent with significant acute toxicity and risk of death. Journal of MedicalToxicology, 7: 205–212.
Google Scholar
Haberman, C. 2014. Agent Orange’s Long Legacy, for Vietnam and Veterans. New York Times.
Google Scholar
Infante-Castillo, R., Hernandez-Rivera S. 2012. Predicting Heats of Explosion of Nitroaromatic Compounds through NBO Charges and 15N NMR Chemical Shifts of Nitro Groups. Advances in Physical Chemistry, vol. 2012.
Google Scholar
Kulkarni, M., Chaudhari, A. 2007. Microbial remediation of nitro-aromatic compounds: An overview. Journal of Environmental Management, 85: 496–512.
Google Scholar
Kumar A., Pandith, A., Seok-Kong, K. 2016. Pyrenebutylamidopropylimidazole as a multi-analyte sensor for 3,5-dinitrosalicylic acid and Hg2+ ions. Journal of Luminescence, 172: 309–316.
Google Scholar
Lenke H., Knackmuss, H.J. 1992. Initial hydrogenation during catabolism of picric acid by Rhodococcuserythropolis HL 24-2. Applied EnvironmentalMicrobiology, 58: 2933–2937.
Google Scholar
Lipczynska-Kochany, E. 1992. Degradation of nitrobenzene and nitrophenols by means of advanced oxidation processes in a homogeneous phase: Photolysis in the presence of hydrogen peroxide versus the Fenton reaction. Chemosphere, 24: 1369–1380.
Google Scholar
Mathieu, D., Alaime, T. 2015. Impact sensitivities of energetic materials: Exploring the limitations of a model based only on structural formulas. Journal of Molecular Graphics and Modelling, 62: 81–86.
Google Scholar
Maza M., Pajot, H.F., Amoroso, M.J., Yasem, M.G. 2015. In-vitro degradation of Czapek and molasses amended post-harvest sugarcane residue by lignocellulolytic fungal strains. International Biodeterioration and Biodegradation, 104: 118–122.
Google Scholar
Nousiainen P., Kontro, J., Manner, H. 2014. Phenolic mediators enhance the manganese peroxidase catalyzed oxidation of recalcitrant lignin model compounds and synthetic lignin. Fungal Genetic Biology, 72: 137–149.
Google Scholar
Price, R.A., Pennington, J.C., Neumann, D., Hayes, C.A., Larson S.L. 1997. Technical Report EL-97–11 US Army Engineer Waterways Experiment Station, Vicksburg.
Google Scholar
Rezaei, B. 2010. Using of multi-walled carbon nanotubes electrode for adsorptive stripping voltammetric determination of ultratrace levels of RDX explosive in the environmental samples. Journal of Hazardous Materials, 83: 138–144.
Google Scholar
Sekhar, P.K., Wignes, F. 2016. Trace detection of research department explosive (RDX) using electrochemical gas sensor. Journal of Sensors, 227: 185–190.
Google Scholar
Shen, J., Zhang, J., Zuo, Y. 2009. Biodegradation of 2,4,6-trinitrophenol by Rhodococcus sp. isolated from a picric acid-contaminated soil. Journal of Hazardous Materials, 163: 1199–1206.
Google Scholar
Singh, R.L., Singh, P.K., Singh, R.P. 2015. Enzymatic decolorization and degradation of azodyes – A review. International Biodeterioration, 104: 21–31.
Google Scholar
Spain J. 1995. Biodegradation of nitroaromatic compounds. Annual Review in Microbiology, 49: 523–555.
Google Scholar
Spain, J., Hughes, J., Knackmuss, H-J. 2000. Biodegradation of nitroaromatic compounds and explosives. Lewis Publishers, pp. 213–234.
Google Scholar
Tashes, F., Bumpus, J., Aust, S. 1990. Biodegradation of TNT (2,4,6-trinitrotoluene) by Phanerochaete chrysosporium. Applied and environmental microbiology. 56: 1666–1671.
Google Scholar
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